Search by meaning, not just keywords: describe the product or the hazard and we find matching recalls even when the official notice uses different words. Brand names and model numbers work too.
Latest recalls
35,021 found- Stop using nowConsumer product

5-Drawer Dressers Recalled Due to Risk of Serious Injury or Death from Tip-Over and Entrapment Hazards; Violate Mandatory Standard for Clothing Storage Units; Sold on Amazon by KAIFAM
KAIFAM recalls 5-drawer dressers sold on Amazon due to tip-over and entrapment risks. Stop use if unanchored and contact KAIFAM for a full refund.
KAIFAMJul 30, 2026 - Stop using nowConsumer product

15-Drawer Dressers Recalled Due to Risk of Serious Injury or Death from Tip-Over and Entrapment Hazards; Violate Mandatory Standard for Clothing Storage Units; Sold on Amazon by Enhomee-Direct
EnHomee 15-Drawer Dressers sold before April 10, 2026, may tip over and trap children, causing serious injury or death. Stop using if not wall-anchored.
EnHomeeJul 30, 2026 - UnratedDrug
BioSpectra, Inc. recalls Biospectra Tris/Tromethamine, USP, GMP, API Grade, Manufactured at 100 Majestic Way, Bangor, PA 18013, NDC 64173-101-25
BioSpectra recalls 200 kg of Tris/Tromethamine, USP, GMP, API Grade due to failed stability specifications. Check lot TRIS-E04-0226-0016.
BioSpectraJul 29, 2026 - Stop using nowVehicle
GRAND DESIGN LINEAGE (2026) recall — Equipment
Grand Design recalls certain 2026-2027 Lineage motorhomes due to incorrect rear tire pressure labels, which can cause overinflation and tire failure.
Grand DesignJul 29, 2026 - Lower riskMedical device
Fresenius Medical Care Renal Therapies Group, LLC recalls CombiSet Hemodialysis Blood Tubing Set with Attached Priming Set and Transducer Protectors; Model Number: 03-2522-1;
Fresenius Medical Care recalls CombiSet hemodialysis tubing sets with model 03-2522-1. Review instructions to ensure safe use; no immediate action needed but check for proper handling.
Fresenius Medical CareJul 29, 2026 - Use cautionMeat & poultry
FSIS Issues Public Health Alert for Steak Burrito Product Due to Misbranding and Undeclared Allergen
USDA FSIS recalls Red's Steak Cilantro Lime Burrito products due to undeclared egg allergen. Consumers urged not to consume; products should be discarded or returned.
Red's All NaturalJul 29, 2026 - Use cautionMedical device
Nova Biomedical Corporation recalls StatStrip Glucose and B- Ketone meter. Model No: 63683. Glucose test system.
Nova Biomedical recalls StatStrip Glucose and Ketone meters (model 63683) due to software error causing patient data mismatches. This may lead to incorrect glucose results being recorded for the wrong patient, risking inappropriate treatment for critically ill patients.
Nova BiomedicalJul 29, 2026 - Stop using nowMedical device
Windstone Medical Packaging, Inc. recalls AMS Convenience Kit: DSAEK Pack - RX, Part Number AMS12394B
Windstone Medical recalls AMS Convenience Kit (DSAek Pack) with possible blue break-off parts that may detach during use. Affected units include specific lot numbers from 2022-2023. Stop using immediately to avoid potential injury.
Windstone MedicalJul 29, 2026 - Lower riskMedical device
Cardinal Health 200, LLC recalls Presource Packs Containing CliniClean Pericare Wipes within BD Urinary Catheter Trays: 1) KIT, ROBOTIC HYST , Catalog
Cardinal Health recalls Presource Packs containing CliniClean Pericare Wipes that may be contaminated with manufacturing lubricant, risking skin irritation or mild inflammation if used on patients.
Cardinal HealthJul 29, 2026 - Lower riskMedical device
Diagnostica Stago, Inc. recalls STA Staclot Protein S, Model/Catalog Number: 00746-Reagent Lot number 273074; qualitative and quantitative factor
Diagnostica Stago recalls STA Staclot Protein S reagent lot 273074 due to potential QC value drift during 4-hour stability period. Affected units may give inaccurate test results.
Diagnostica StagoJul 29, 2026 - Lower riskMedical device
Healthmark Industries Co., Inc. recalls healthmark ProChek-II, Model Number PT-313, PT-201-12
Healthmark recalls ProChek-II devices with specific serial numbers due to expired ingredients causing false test results. Affected units may show inaccurate results, potentially leading to incorrect health decisions.
HealthmarkJul 29, 2026 - Lower riskDrug
Shilpa Medicare Limited recalls PEMRYDI RTU(pemetrexed injection), 500 mg/50 mL (10 mg/mL), Single-dose vial, Rx only, Manufactured by: Zydus
Shilpa Medicare recalls PEMRYDI RTU (pemetrexed injection) due to green discoloration in vials. This may indicate contamination. Check vial color before use.
Shilpa MedicareJul 29, 2026 - Lower riskDrug
Apollo Care, LLC recalls SEMAGLUTIDE 9mg (4.5 mg/mL), 2 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801
Apollo Care recalls SEMAGLUTIDE 9mg vials due to particulate matter that could cause injection site reactions. Affected vials have specific NDC and lot numbers. Consumers should contact Apollo Care for details.
Apollo CareJul 29, 2026 - Stop using nowDrug
Prestige Brands Holdings recalls CLEAR EYES Maximum Itchy Eye Relief, 0.5 fl oz (15 mL) per dropper bottle, Sterile, Dist. by Medtech Products Inc.,
Prestige Brands recalls Clear Eyes Maximum Itchy Eye Relief drops due to lack of sterility assurance. Check your lot number and expiration date.
Clear EyesJul 29, 2026 - Lower riskFood
Kerry, Inc recalls KC Everyday Mac & Cheese, 3lb x 6. Item # 20609055. 6 - 3 lb pouches, Net Wt: 18 lb. (8.16Kg). Fully Cooked. Keep
Kerry recalls 6-pack of 3lb KC Everyday Mac & Cheese (item #20609055) due to undeclared egg allergen. Consumers should check lot numbers 0011849964, 0011988192, 0012085206 for affected products.
KerryJul 29, 2026 - Use cautionVehicle
FORD F-250 SD (2023) recall — Back Over Prevention
Ford recalls certain F-150 and F-250 SD vehicles due to a rearview camera image obstruction. Check if your VIN is affected and get a free software update.
FordJul 29, 2026 - Use cautionVehicle
FORD MUSTANG MACH E (2025) recall — Structure
Ford is recalling certain 2023-2025 Mustang Mach E vehicles due to rear quarter window trim that may detach, creating road hazards and crash risks. Owners must contact Ford for free inspection and replacement.
FordJul 28, 2026 - Lower riskMedical device
Ventec Life Systems, Inc. recalls REF: HF2POSTD HomeFill Oxygen System HomeFill cylinder D with CGA870 Compatible Post Valve
Ventec Life Systems recalls HomeFill oxygen cylinders with CGA870 Post Valve that lack required medical gas labeling. Consumers should check serial numbers listed to determine if affected.
Ventec Life SystemsJul 28, 2026 - Lower riskFood
Wonton Specialists recalls Wonton Specialist Inc. Wonton Skin, 16 oz - packaged in foam tray overwrapped with clear plastic
Wonton Specialists recalls 16 oz wonton skin with undeclared FD&C Red 40 dye. Consumers should check packaging for foam tray and clear plastic wrap.
Wonton SpecialistsJul 28, 2026 - Stop using nowDrug
Regeneron Pharmaceuticals Inc recalls Libtayo (cemiplimab-rwlc) Injection, 350 mg/7 mL (50 mg/mL), For Intravenous Infusion After Dilution, Single-Dose Vial,
Regeneron recalls Libtayo (cemiplimab-rwlc) injections due to lack of sterility assurance. This could lead to infections if used improperly. Affected units have specific lot numbers and expiration dates.
RegeneronJul 28, 2026 - Lower riskFood

529 COMMERCE, LLC recalls Aquafaba Powder, Vegan Replacement, NET WT. 4 oz (113g) and 12 0z (340g), Resealable stand-up matte foil pouch with
529 Commerce recalls vegan aquafaba powder products due to undeclared egg content. Consumers should check UPCs and best-by dates for affected lots.
529 CommerceJul 28, 2026 - Lower riskFood
FlavorsandColor.Com recalls Honeyville YELLOW COLOR 1 GALLON NFI: WATER, FD&C YELLOW #5, FD&C YELLOW #6, CITRIC ACID, AND SODIUM BENZOATE.
FlavorsandColor recalls Honeyville Yellow Color 1 Gallon due to undeclared Red 40. This may cause allergic reactions in sensitive individuals. Check product details for affected lots.
FlavorsandColorJul 28, 2026 - Lower riskMedical device
HeartSine Technologies Ltd recalls HeartSine samaritan PAD (Public Access Defibrillator); HeartSine SAM 350P 350P US Device, US English - 2 Min CPR UDI-DI
HeartSine iECG is a portable, wearable ECG monitor that provides continuous heart rhythm monitoring for patients with cardiac conditions.
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24E90015275A24 24E90015277A24 24E90001278A24 24E90001281A24 24E90001283A24 24E90001284A24 24E90001256A24 24E90000644A24 24E90000645A24 24E90015280A24 24E90001280A24 24E90000648A24 24E90000646A24 24E90001253A24 24E90000639A24 24E90000640A24 24E90000636A24 24E90000635A24 24E90001287A24 24E90000642A24 24E90001285A24 24E90000643A24 24E90001286A24Jul 27, 2026 - Stop using nowFood
Elegant Foods, LLC recalls Pecorino Toscano D.O.P. STAGIONATO cheese wheels. Product of Italy. Each cheese wheel is approximately 3-4 lbs. Wheels
Elegant Foods recalls Italian Pecorino Toscano D.O.P. STAGIONATO cheese wheels due to potential Listeria contamination from condensation in coolers. Keep refrigerated and check for wax rind.
Elegant FoodsJul 27, 2026 - Lower riskMedical device
restor3d Inc. recalls Kinos Axiom Total Ankle System with Axiom PSR, Flat-cut (Cut Guide), REF: 5831-9006
restor3d recalls Kinos Axiom Total Ankle Systems with incorrect patient-specific cutting guides that may cause delayed surgery, poor implant alignment, or revision surgery. Affected units have specific serial numbers and reference codes.
restor3dJul 27, 2026 - Lower riskMedical device
HeartSine Technologies Ltd recalls HeartSine SAM 350P 350P US Device, US English - 2 Min CPR UDI-DI codes: 0506016712067 350P US Device, US English
HeartSine 350P US Device, US English (American Airlines) - 2 Min CPR
HeartSineJul 27, 2026 - Use cautionVehicle
KENWORTH T680 (2027) recall — Electrical System
PACCAR recalls certain 2027 Kenworth T680 trucks with contaminated power distribution centers that may cause loss of lighting, wipers, ABS, or drive power, increasing crash risk. Owners must have PDC boxes replaced free by dealers.
KenworthJul 27, 2026 - Stop using nowFood
Centric Compounding LLC recalls Tri-Immune Boost (Glutathione: 200 mg, Ascorbic Acid: 200 mg, Zinc: 2.5 mg), 30 mL vial, Rx only, Centric Compounding,
Centric Compounding LLC recalls specific lots of Tri-Immune Boost vials due to microbial contamination and out-of-spec bacterial endotoxin levels.
Centric CompoundingJul 27, 2026 - Stop using nowMedical device
QUANTUM OPS Inc recalls Brand Name: ADAPTABLE Beach Chair Product Name: Beach Chair surgical patient positioner Model/Catalog Number:
ADAPTABLE Beach Chair surgical patient positioners with inadequate welds in the head positioning system are recalled. These devices risk patient injury during surgery. Stop using immediately and contact the manufacturer for a replacement.
ADAPTABLEJul 24, 2026 - Lower riskMedical device
Onkos Surgical, Inc. recalls Onkos Surgical Inc. My3D Personalized Pelvic Implant, Porous, Left REF PV-ACREC-04M
Onkos Surgical recalls My3D Personalized Pelvic Implant, Porous, Left REF PV-ACREC-04M due to being mixed up with incorrect customers. This affects 1 implant sold nationwide in North Carolina and California.
Onkos SurgicalJul 24, 2026
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